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1.
Curr Top Med Chem ; 11(3): 317-30, 2011.
Artículo en Inglés | MEDLINE | ID: mdl-21320060

RESUMEN

The recognition that malfunction of the microtubule (MT) associated protein tau is likely to play a defining role in the onset and/or progression of a number of neurodegenerative diseases, including Alzheimer's disease, has resulted in the initiation of drug discovery programs that target this protein. Tau is an endogenous MT-stabilizing agent that is highly expressed in the axons of neurons. The MT-stabilizing function of tau is essential for the axonal transport of proteins, neurotransmitters and other cellular constituents. Under pathological conditions, tau misfolding and aggregation results in axonal transport deficits that appear to have deleterious consequences for the affected neurons, leading to synapse dysfunction and, ultimately, neuronal loss. This review focuses on both progress and unresolved issues surrounding the development of novel therapeutics for the treatment of neurodegenerative tauopathies, which are based on (A) MT-stabilizing agents to compensate for the loss of normal tau function, and (B) small molecule inhibitors of tau aggregation.


Asunto(s)
Multimerización de Proteína/efectos de los fármacos , Tauopatías/tratamiento farmacológico , Tauopatías/metabolismo , Proteínas tau/metabolismo , Animales , Humanos , Unión Proteica/efectos de los fármacos , Moduladores de Tubulina/química , Moduladores de Tubulina/farmacología , Moduladores de Tubulina/uso terapéutico , Proteínas tau/química
2.
J Med Chem ; 35(13): 2347-54, 1992 Jun 26.
Artículo en Inglés | MEDLINE | ID: mdl-1619614

RESUMEN

A series of isomeric 2',3'-dideoxynucleosides which contains a modified carbohydrate moiety has been prepared. This class of compounds was designed to mimic the activity of known anti-HIV dideoxynucleosides, while imparting enhanced chemical and enzymatic stability. Isonucleosides containing the standard heterocyclic bases (A, C, G, T) were synthesized via nucleophilic addition of the base to an isomeric sugar unit. Modified derivatives were generated by manipulation of the intact isonucleoside. Two of the compound prepared, iso-ddA (1) and iso-ddG (6), exhibit significant and selective anti-HIV activity, as well as beneficial hydrolytic stability.


Asunto(s)
Antivirales/síntesis química , Didesoxinucleósidos/síntesis química , VIH-1 , Antivirales/farmacología , Células Cultivadas , Cromatografía Liquida , Didesoxinucleósidos/farmacología , Estabilidad de Medicamentos , Productos del Gen gag/biosíntesis , VIH-1/fisiología , Humanos , Isomerismo , Monocitos/metabolismo , Análisis Espectral , Replicación Viral/efectos de los fármacos
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